Investigating the bifunctional electrocatalytic activity of nickel oxide/nitrogen-doped reduced graphene oxide nanocomposite for zinc-air battery application

IF 2.6 4区 化学 Q3 ELECTROCHEMISTRY
Habu Abba, Magaji Ladan, Haruna Musa, Ibrahim Tajo Siraj, Ahmad Muhammad Yamani, Abdulfatah Shehu Muhammad, Nura Muhammad Kwalam, Abdul-Rahman A. Abdul, Ayuba Abdullahi Muhammad, Shehu Habibu, Md. Shalauddin, Nasar Mansir, Wan Jeffrey Basirun, Mustapha Balarabe Idris
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Abstract

The performance of electrically rechargeable zinc-air batteries (ErZAB) depends on the efficiency of bifunctional electrocatalysts. Herein, four different forms of the nickel oxide/nitrogen-doped reduced graphene oxide (NiO/rGO), with various amounts of the Acacia Ataxacantha leaves extract, were synthesized by a hydrothermal method. The effect of the extract loading on the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is reported. The energy dispersive X-ray spectra confirm that the plant extract can act as a dopant for nitrogen and reductant for the graphene oxide, whereas the field emission scanning electron microscopic (FE-SEM) images demonstrate that the NiO nanoparticles were uniformly dispersed onto the surface of the rGO thereby providing greater number of active sites for electrocatalytic activity. The electrochemical characterization reveals that the doping of the N improves the bifunctional electrocatalytic activity of NiO-rGO nanocomposite. Furthermore, the ORR and OER onset potential were found to decrease and increase with an increase in the loading level of the plant extract respectively. It was found that 7.5 mL of the plant extract is the optimum loading level to achieve the highest ORR and OER electrocatalytic activities. Furthermore, battery testing indicated that the bifunctional electrocatalyst showed outstanding charge-discharge cycle performances, with its voltage polarization exhibiting a 0.25% decrease in discharge and a 1.4% increase in charge after 50 charge-discharge cycles.

研究了氧化镍/氮掺杂还原氧化石墨烯纳米复合材料在锌空气电池中的双功能电催化活性
电可充电锌空气电池(ErZAB)的性能取决于双功能电催化剂的效率。本文采用水热法合成了四种不同形式的氧化镍/氮掺杂还原氧化石墨烯(NiO/rGO),并添加了不同量的金合欢叶提取物。报道了萃取物负载对氧还原反应(ORR)和析氧反应(OER)的影响。能量色散x射线光谱证实,植物提取物可以作为氮的掺杂剂和氧化石墨烯的还原剂,而场发射扫描电镜(FE-SEM)图像表明,NiO纳米颗粒均匀地分散在还原氧化石墨烯表面,从而为电催化活性提供了更多的活性位点。电化学表征表明,N的掺杂提高了NiO-rGO纳米复合材料的双功能电催化活性。此外,ORR和OER启动电位分别随着植物提取物负荷水平的增加而降低和增加。结果表明,7.5 mL的植物提取物是获得最高ORR和OER电催化活性的最佳负载水平。此外,电池测试表明,双功能电催化剂具有出色的充放电循环性能,在50次充放电循环后,其电压极化放电减少0.25%,充电增加1.4%。
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来源期刊
CiteScore
4.80
自引率
4.00%
发文量
227
审稿时长
4.1 months
期刊介绍: The Journal of Solid State Electrochemistry is devoted to all aspects of solid-state chemistry and solid-state physics in electrochemistry. The Journal of Solid State Electrochemistry publishes papers on all aspects of electrochemistry of solid compounds, including experimental and theoretical, basic and applied work. It equally publishes papers on the thermodynamics and kinetics of electrochemical reactions if at least one actively participating phase is solid. Also of interest are articles on the transport of ions and electrons in solids whenever these processes are relevant to electrochemical reactions and on the use of solid-state electrochemical reactions in the analysis of solids and their surfaces. The journal covers solid-state electrochemistry and focusses on the following fields: mechanisms of solid-state electrochemical reactions, semiconductor electrochemistry, electrochemical batteries, accumulators and fuel cells, electrochemical mineral leaching, galvanic metal plating, electrochemical potential memory devices, solid-state electrochemical sensors, ion and electron transport in solid materials and polymers, electrocatalysis, photoelectrochemistry, corrosion of solid materials, solid-state electroanalysis, electrochemical machining of materials, electrochromism and electrochromic devices, new electrochemical solid-state synthesis. The Journal of Solid State Electrochemistry makes the professional in research and industry aware of this swift progress and its importance for future developments and success in the above-mentioned fields.
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